Predicting recurrence in patients with breast cancer from cumulative laboratory results: a new technique for the application of time series analysis.

Author:

Winkel P,Bentzon M W,Statland B E,Mouridsen H,Sheike O

Abstract

Abstract We followed the cases of 26 consecutive postmenopausal patients operated on for primary breast cancer. Serum specimens were obtained each month for 1.5 years and stored at -80 degrees C until assayed for carcinoembryonic antigen (CEA) and other quantities. Ten patients developed recurrence, while 16 qualified as controls (no clinical recurrence for at least 1.7 years after the last venipuncture). Using the homeostatic autoregressive time series model, modified by us to be particularly sensitive to sustained deviations from the mean, we detected four recurrences by CEA without having any falsely positive alarms. Group-based reference limits and application of the unmodified homeostatic model were less effective (fewer detected and shorter lead time). Simulation studies, involving use of a mathematical model relating CEA concentration to tumor growth and using parameters estimated from patient data, verified this and indicated that at least five stable baseline values are needed to detect 100% of recurrences before they are detected by the group-based limit.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Intraindividual reference values;Clinical Chemistry and Laboratory Medicine (CCLM);2004-01-05

2. Application of time series analysis in the clinical setting;Scandinavian Journal of Clinical and Laboratory Investigation;1995-01

3. Individual reference ranges of CA 15—3, MCA and CEA in recurrence of breast cancer;Scandinavian Journal of Clinical and Laboratory Investigation;1995-01

4. A novel method for monitoring high-risk breast cancer with tumor markers: CA 15.3 compared to CEA and TPA;Annals of Oncology;1993-12

5. Using autoregressive and random walk models to detect trends and shifts in unequally spaced tumour biomarker data;Statistics in Medicine;1993-02

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